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1.
Paolo Aluffi 《Rendiconti del Circolo Matematico di Palermo》1938,62(1):3-26
We obtain a precise relation between the Chern–Schwartz–MacPherson class of a subvariety of projective space and the Euler characteristics of its general linear sections. In the case of a hypersurface, this leads to simple proofs of formulas of Dimca–Papadima and Huh for the degrees of the polar map of a homogeneous polynomial, extending these formula to any algebraically closed field of characteristic \(0\), and proving a conjecture of Dolgachev on ‘homaloidal’ polynomials in the same context. We generalize these formulas to subschemes of higher codimension in projective space. We also describe a simple approach to a theory of ‘polynomial Chern classes’ for varieties endowed with a morphism to projective space, recovering properties analogous to the Deligne–Grothendieck axioms from basic properties of the Euler characteristic. We prove that the polynomial Chern class defines homomorphisms from suitable relative Grothendieck rings of varieties to \(\mathbb{Z }[t]\). 相似文献
2.
3.
Crystals of 1,6-8, 13-bis-oxido-[14]-annulene are monoclinic, a = 9,29, b = 9,74, c = 11,46 Å, β = 90,0°, space group P 21/c, with 4 molecules in the unit cell. The structure has been solved by direct methods and refined by full-matrix least-squares analysis of three-dimensional intensity data. The cis-configuration of the two oxygen bridges is confirmed, and the observed molecular parameters are in full accord with the aromatic properties of the molecule. 相似文献
4.
Vincenzo Bertini Angela De Munno Paolo Pelosi Piero Pino 《Journal of heterocyclic chemistry》1968,5(5):621-624
Cycloaddition of fulminic acid to 1-butyn-3-ol gave a mixture of 5-α-hydroxyethylisoxazole (I) and 4-α-hydroxyethylisoxazole (II) in the ratio 9:1. By the dehydration of 1, 5-vinylisoxazole (III) was obtained. Compound III has also been prepared by cyclization of 4-penten-2-ynal as well as its diethylacetal with hydroxylamine hydrochloride; in both instances no isomers have been obtained. Compound III spontaneously polymerizes even at room temperature yielding a polymer still containing isoxazole rings. 相似文献
5.
Enantiomeric separation of some selected acidic compounds of pharmaceutical interest belonging to the group of non-steroidal anti-inflammatory drugs were separated by capillary electrochromatography employing silica based glycopeptide antibiotic stationary phases, namely vancomycin or a teicoplanin derivatives (Hepta-Tyr). The vancomycin stationary phase allowed to achieve the chiral resolution of some racemic studied compounds only using mobile phases containing ammonium formate at a relatively low pH 2.5-3.5 and acetonitrile. Employing the teicoplanin derivative stationary phase, good enantiomeric resolution was achieved eluting with mobile phases containing sodium phosphate pH 6-acetonitrile. Enantiomers were moved to the detector because a relatively high reversed electroosmotic flow (due to the positive charge of the stationary phase) and to the electrophoretic mobility of analytes. 相似文献
6.
In order to use micellar electrokinetic chromatography to determine the proteolytic activity of different proteinases simultaneously present in physiological fluids, the technique must be able to separate mixtures of substrates with closely related structures. In an attempt to determine the best electrophoretic conditions for resolving six p-nitroanilide peptides used as synthetic substrates of the elastolytic enzymes (human neutrophil elastase, cathepsin G, Pseudomonas aeruginosa elastase) most commonly involved in pulmonary diseases, we investigated the efficiency of ionic and nonionic surfactants in achieving the separation of this complex mixture. The results presented here show that, of all the electrophoretic systems tested, 30 mM sodium tetraborate, pH 9.3, containing 25 mM Brij 35 as micellar agent offered the best performance; the separation efficiency of peptides is greater than that obtained with other reagents and all peaks are baseline resolved and unambiguously identifiable. Analysis of the micelle-solute interaction with the surfactants investigated allowed better definition of the mechanism involved in the distribution of these peptides to the micelles and identification of some structural features that determined the magnitude of the micelle peptide complex formation. 相似文献
7.
Fluorocarbons containing higher halogens have the potency of breaking certain hydrogen bonds in solutions. The relative strength of this potency varies in the series F < Cl < Br < I and the presence of hydrogen atoms in the fluorocarbon increases it. There is a striking parallelism between the hydrogen bond breaking and the anaesthetic potency of these molecules. It is suggested that the breaking of hydrogen bonds is an important step in the mechanism of anaesthesia. 相似文献
8.
Paolo Davoli 《Tetrahedron》2005,61(18):4427-4436
The enantioselective total synthesis of the actin-targeting metabolite (−)-microcarpalide is described. Key steps include ring-closing metathesis (RCM) for the final construction of the 10-membered lactone framework and stereoselective homologation of boronic esters for the insertion of all stereocentres with the desired absolute configuration. In particular, the acidic fragment was prepared in seven steps from a suitable chiral bromomethane boronate by means of two sequential stereoselective homologations to install the two stereocentres with the correct final R stereochemistry, employing (−)-pinanediol as the chiral director. Subsequent elaboration to the required C7 backbone entailed nucleophilic displacement with a vinyl Grignard reagent, oxidative cleavage of the boronic scaffold and protection-deprotection manipulations. Interestingly, when the tribenzyloxy diene ester resulting from DCC-mediated coupling of the two key synthons was subjected to RCM in the presence of Grubbs' catalyst, the reaction proceeded stereoselectively to yield the desired trans oxecin-2-one, albeit with poor conversion. 相似文献
9.
Gian Angelo Vaglio Paolo Volpe Lorenza Operti 《Journal of mass spectrometry : JMS》1982,17(12):617-619
The negative ion chemical ionization mass spectra, with ammonia and methane as reagent gases, of the (η6-arene)Cr(CO)3 complexes, where the arene is C6H5COCH3, C6H5COC2H5, C6H5COC3H7, C6H5COC(CH3)3, 2-CH3C6H4COC3H7, C6H5COOCH3, C6H5CH3, 1,3,5-(CH3)3C6H3 and C6H5CH2COC2H5, are reported. Similar behaviour is observed with the two reagent gases, but ammonia shows a much higher abundance for the ions produced by reactions of [NH2]? with sample molecules. The compounds containing the C6H5CO group display an abundant [M]? ˙, whereas the other compounds exhibit [M? H]? as base peak, produced by ion/molecule reactions. A comparison of the negative ion chemical ionization mass spectra of the (η6-arene)Cr(CO)3 complexes with those of the corresponding ligands shows the strong electron withdrawing power of the Cr(CO)3 group in the gas phase. 相似文献
10.
Gian Paolo Chiusoli Mirco Costa Luciano Pallini Giuliana Terenghi 《Transition Metal Chemistry》1982,7(6):304-306
Summary In presence of nickel or palladium catalysts, nucleophiles can attack vinylcyclopropanes with concomitant ring cleavage. With palladium catalysts in presence of appropriate substituents the terminal carbon atom of the resulting open chain is able to add to two molecules of a conjugated diene giving rise to long-chain unsaturated compounds. 相似文献